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rs794727830

From SNPedia

Orientationminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs794727830(-;-)
Make rs794727830(-;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position215648607
GeneUSH2A
is asnp
is mentioned by
dbSNPrs794727830
ebirs794727830
HLIrs794727830
Exacrs794727830
Varsomers794727830
Maprs794727830
PheGenIrs794727830
hapmaprs794727830
1000 genomesrs794727830
hgdprs794727830
ensemblrs794727830
gopubmedrs794727830
geneviewrs794727830
scholarrs794727830
googlers794727830
pharmgkbrs794727830
gwascentralrs794727830
openSNPrs794727830
23andMers794727830
23andMe allrs794727830
SNP Nexus

SNPshotrs794727830
SNPdbers794727830
MSV3drs794727830
GWAS Ctlgrs794727830
Max Magnitude0
ClinVar
Risk rs794727830(;)
Alt rs794727830(;)
Reference rs794727830(TC;TC)
Significance Pathogenic
Disease Usher syndrome
Variation info
Gene USH2A
CLNDBN Usher syndrome, type 2A
Reversed 1
HGVS NC_000001.10:g.215821949_215821950delGA
CLNSRC
CLNACC RCV000179668.1,